John Greally
@greally.bsky.social
Using genomic information to improve medicine
And we’re the outliers with peculiarities?
February 7, 2026 at 3:05 PM
And we’re the outliers with peculiarities?
Gift link www.nytimes.com/2026/02/06/o...
Opinion | The Finance Industry Is a Grift. Let’s Start Treating It That Way.
www.nytimes.com
February 6, 2026 at 2:10 PM
Gift link www.nytimes.com/2026/02/06/o...
Solid genomics and statistical analyses involved, plus some innovative machine learning designed to bring FNCV information to clinical diagnostics.
The postdoc will be embedded with the @newyorkcrd.bsky.social group, who have an interest in getting FNCVs into translational use.
The postdoc will be embedded with the @newyorkcrd.bsky.social group, who have an interest in getting FNCVs into translational use.
February 5, 2026 at 10:49 PM
Solid genomics and statistical analyses involved, plus some innovative machine learning designed to bring FNCV information to clinical diagnostics.
The postdoc will be embedded with the @newyorkcrd.bsky.social group, who have an interest in getting FNCVs into translational use.
The postdoc will be embedded with the @newyorkcrd.bsky.social group, who have an interest in getting FNCVs into translational use.
This position has 2 years of funding from SFARI to test our findings that indicate an accumulation of functional non-coding variants (FNCVs) in regulatory loci of glutamatergic neurons causing neurodevelopment disorders.
February 5, 2026 at 10:49 PM
This position has 2 years of funding from SFARI to test our findings that indicate an accumulation of functional non-coding variants (FNCVs) in regulatory loci of glutamatergic neurons causing neurodevelopment disorders.
Examples of Departmental strengths include model organism researchers (including Hannes Bülow, Bernice Morrow, Meelad Dawlaty, Julie Secombe), ageing research (Jan Vijg) and population genetics (Srilakshmi Raj), and is the home for the research arm of the @newyorkcrd.bsky.social.
February 5, 2026 at 10:15 PM
Examples of Departmental strengths include model organism researchers (including Hannes Bülow, Bernice Morrow, Meelad Dawlaty, Julie Secombe), ageing research (Jan Vijg) and population genetics (Srilakshmi Raj), and is the home for the research arm of the @newyorkcrd.bsky.social.
The goal is to understand how non-coding sequence variation may cause intellectual disability, improving our ability to give families answers when they have a child with this condition.
Anyone interested should reach out to me directly. We will officially post the position soon.
Anyone interested should reach out to me directly. We will officially post the position soon.
January 30, 2026 at 8:01 PM
The goal is to understand how non-coding sequence variation may cause intellectual disability, improving our ability to give families answers when they have a child with this condition.
Anyone interested should reach out to me directly. We will officially post the position soon.
Anyone interested should reach out to me directly. We will officially post the position soon.
The applicant should have the ability to work with large genomic datasets, and learn/apply statistical and machine learning approaches. They will be co-mentored by Srilakshmi Raj. Start date May 1 2026, we need to fill the position soon. 2/3
January 30, 2026 at 8:00 PM
The applicant should have the ability to work with large genomic datasets, and learn/apply statistical and machine learning approaches. They will be co-mentored by Srilakshmi Raj. Start date May 1 2026, we need to fill the position soon. 2/3
The term 'junk DNA', used by Susumu Ohno in 1972, has no modern validity over a half century later. This 98.8% of the genome is what regulates gene expression, it's fascinating.
January 28, 2026 at 7:27 PM
The term 'junk DNA', used by Susumu Ohno in 1972, has no modern validity over a half century later. This 98.8% of the genome is what regulates gene expression, it's fascinating.
We're using it. Nobody should expect a step forward to complete a long journey, but this is a significant step forward and should be celebrated.
We only understand the 1.2% of the human genome that encodes genes. AlphaGenome is a tool towards understanding the remaining 98.8%.
We only understand the 1.2% of the human genome that encodes genes. AlphaGenome is a tool towards understanding the remaining 98.8%.
January 28, 2026 at 6:07 PM
We're using it. Nobody should expect a step forward to complete a long journey, but this is a significant step forward and should be celebrated.
We only understand the 1.2% of the human genome that encodes genes. AlphaGenome is a tool towards understanding the remaining 98.8%.
We only understand the 1.2% of the human genome that encodes genes. AlphaGenome is a tool towards understanding the remaining 98.8%.
You're not ready for grant applications yet, right? Just manuscripts?
January 26, 2026 at 3:31 PM
You're not ready for grant applications yet, right? Just manuscripts?
A reminder that history is rewritten every day. There is no Irish genome. Irishness is not genetic.
www.bbc.com/sport/athlet...
www.bbc.com/sport/athlet...
January 26, 2026 at 3:12 PM
A reminder that history is rewritten every day. There is no Irish genome. Irishness is not genetic.
www.bbc.com/sport/athlet...
www.bbc.com/sport/athlet...
Plus this commercial prenatal testing to create "superbabies" is all unapologetic eugenics, disgusting and vile
January 22, 2026 at 4:55 PM
Plus this commercial prenatal testing to create "superbabies" is all unapologetic eugenics, disgusting and vile